A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1073826



Internal ID19325554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:186553745..186557246hg38UCSC Ensembl
chr4:187474899..187478400hg19UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg383502
hg193502
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3772599
SamplesKWP1
Known GenesMTNR1A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1073826
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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